Basic information

Biomarker: LSD1

Histology type: endometrioid endometrial carcinoma

Cohort characteristics

Country: China

Region: Harbin

Followed up time :

Subgroup 1 name : Negative

Subgroup 1 number: 59

Subgroup 2 name: Positive

Subgroup 2 number: 147

Total number Group I Group I number Group II Group II number Group III Group III number Group IV Group IV number
355 EEA 260 benign endometrial lesion specimens 50 normal endometrium specimens 45

Sample information

Conclusion: Overexpression of LSD1 may contribute to the progression of EEA and may thus serve as a new biomarker to predict the prognosis of EEA.

Sample type : tissue

Sample method: Immunohistochemistry/Real-Time PCR

Expression pattern : Overexpression

Expression elevation: The staining intensity was described by scores between 0 and 3 (0 = no reaction, 1 = low, 2 = moderate, 3 = strong). Accordingly, the number of positive cell nuclei was counted and scored between 0 and 4 (0 = no positive cell nuclei,1 = ≤10% positive cell nuclei, 2 = 10%-50% positive cell nuclei, 3 = 51-80% positive cell nuclei, 4 = ≧80% positive cell nuclei). The product of staining intensity and percentage of positive cell nuclei resulted in a score between 0 and 12. Each sample was categorized by this rating score. Scores of 4 or greater were considered positive.

Disease information

Statictics: cutoff<60;cutoff>60

Subgroup 1 age: 36;74

Subgroup 2 age: 23;73

Related information

Funtion Uniprot: Histone demethylase that can demethylate both 'Lys-4' (H3K4me) and 'Lys-9' (H3K9me) of histone H3, thereby acting as a coactivator or a corepressor, depending on the context (PubMed:15620353, PubMed:15811342, PubMed:16140033, PubMed:16079794, PubMed:16079795, PubMed:16223729). Acts by oxidizing the substrate by FAD to generate the corresponding imine that is subsequently hydrolyzed (PubMed:15620353, PubMed:15811342, PubMed:16079794, PubMed:21300290). Acts as a corepressor by mediating demethylation of H3K4me, a specific tag for epigenetic transcriptional activation. Demethylates both mono- (H3K4me1) and di-methylated (H3K4me2) H3K4me (PubMed:15620353, PubMed:20389281, PubMed:21300290, PubMed:23721412). May play a role in the repression of neuronal genes. Alone, it is unable to demethylate H3K4me on nucleosomes and requires the presence of RCOR1/CoREST to achieve such activity (PubMed:16140033, PubMed:16079794, PubMed:16885027, PubMed:21300290, PubMed:23721412). Also acts as a coactivator of androgen receptor (AR)-dependent transcription, by being recruited to AR target genes and mediating demethylation of H3K9me, a specific tag for epigenetic transcriptional repression. The presence of PRKCB in AR-containing complexes, which mediates phosphorylation of 'Thr-6' of histone H3 (H3T6ph), a specific tag that prevents demethylation H3K4me, prevents H3K4me demethylase activity of KDM1A (PubMed:16079795). Demethylates di-methylated 'Lys-370' of p53/TP53 which prevents interaction of p53/TP53 with TP53BP1 and represses p53/TP53-mediated transcriptional activation. Demethylates and stabilizes the DNA methylase DNMT1. Required for gastrulation during embryogenesis. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development. Effector of SNAI1-mediated transcription repression of E-cadherin/CDH1, CDN7 and KRT8. Required for the maintenance of the silenced state of the SNAI1 target genes E-cadherin/CDH1 and CDN7 (PubMed:20389281).

UniProt ID: O60341

UniProt Link: https://www.uniprot.org/uniprotkb/O60341/entry

Biological function from UniProt: #Transcription #Transcription regulation

Molecular function from UniProt:

Tissue specificity from UniProt: Ubiquitously expressed.

Subcellular UniProt: #Nucleus

Alternative name from UniProt:

Caution: Was previously reported to interact with ASXL1. However, this publication has been retracted.

Catalytic activity: 2 A + 2 H2O + N6,N6-dimethyl-L-lysyl4-[histone H3] = 2 AH2 + 2 formaldehyde + L-lysyl4-[histone H3]

Activity regulation: The N-terminal sequences of INSM1 and SNAI1 compete with histone H3 for the same binding site and thereby inhibit histone demethylation (in vitro).

Recommended name: Lysine-specific histone demethylase 1A

Gene name from HGNC: KDM1A (AOF2, BHC110, KDM1, KIAA0601, LSD1)

HPA class: Disease related genes Enzymes Human disease related genes Potential drug targets

AlphaFold DB: O60341

AlphaFold Link: https://alphafold.ebi.ac.uk/entry/O60341

Induction: Down-regulated during neural differentiation in neuroblastoma cancer.

HPA link: https://www.proteinatlas.org/ENSG00000004487-KDM1A

Tissue specificity RNA from HPA: Low tissue specificity

Tissue expression from HPA: Ubiquitous nuclear expression.

Single cell type specificity Cell type enhanced (Spermatocytes)

Immune cell specificity: Low immune cell specificity

Subcellular summary HPA Located in Nucleoplasm, Cytosol

Cancer prognostic summary HPA Prognostic marker in liver cancer (unfavorable) and colorectal cancer (favorable)

Pathology link: https://www.proteinatlas.org/ENSG00000004487-KDM1A/pathology

Pathology endo: https://www.proteinatlas.org/ENSG00000004487-KDM1A/pathology/endometrial+cancer

Phenotype ID: 616728

Disease: Cleft palate, psychomotor retardation, and distinctive facial features (CPRF)

Note1: The disease is caused by variants affecting the gene represented in this entry

OMIM link1: https://www.omim.org/entry/616728

HGNC ID: HGNC:29079

HGNC link: https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:29079

Visulization